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The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis
INTRODUCTION: Our aims were to determine whether anion gap normalization time (AGNT) correlates with risk factors related to the severity of diabetic ketoacidosis (DKA) in children, and to characterize AGNT as a criterion for DKA resolution in children admitted with moderate or severe disease. METHO...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275565/ https://www.ncbi.nlm.nih.gov/pubmed/37334219 http://dx.doi.org/10.3389/fped.2023.1198581 |
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author | Lazar, Isaac Wizeman-Orlov, Dorit Hazan, Guy Orbach, Asaf Haim, Alon Cavari, Yuval Feinstein, Yael Neeman, Eitan Hershkovitz, Eli Faingelernt, Yaniv |
author_facet | Lazar, Isaac Wizeman-Orlov, Dorit Hazan, Guy Orbach, Asaf Haim, Alon Cavari, Yuval Feinstein, Yael Neeman, Eitan Hershkovitz, Eli Faingelernt, Yaniv |
author_sort | Lazar, Isaac |
collection | PubMed |
description | INTRODUCTION: Our aims were to determine whether anion gap normalization time (AGNT) correlates with risk factors related to the severity of diabetic ketoacidosis (DKA) in children, and to characterize AGNT as a criterion for DKA resolution in children admitted with moderate or severe disease. METHODS: A ten-year retrospective cohort study of children admitted to the intensive care unit with DKA. We used a survival analysis approach to determine changes in serum glucose, bicarbonate, pH, and anion gap following admission. Using multivariate analysis, we examined associations between patients' demographic and laboratory characteristics with delayed normalization of the anion gap. RESULTS: A total of 95 patients were analyzed. The median AGNT was 8 h. Delayed AGNT (>8 h) correlated with pH < 7.1 and serum glucose >500 mg/dL. In multivariate analysis, glucose >500 mg/dL was associated with an increased risk for delayed AGNT, by 3.41 fold. Each 25 mg/dL elevation in glucose was associated with a 10% increment in risk for delayed AGNT. Median AGNT preceded median PICU discharge by 15 h (8 vs. 23 h). DISCUSSION: AGNT represents a return to normal glucose-based physiology and an improvement in dehydration. The correlation observed between delayed AGNT and markers of DKA severity supports the usefulness of AGNT for assessing DKA recovery. |
format | Online Article Text |
id | pubmed-10275565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102755652023-06-17 The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis Lazar, Isaac Wizeman-Orlov, Dorit Hazan, Guy Orbach, Asaf Haim, Alon Cavari, Yuval Feinstein, Yael Neeman, Eitan Hershkovitz, Eli Faingelernt, Yaniv Front Pediatr Pediatrics INTRODUCTION: Our aims were to determine whether anion gap normalization time (AGNT) correlates with risk factors related to the severity of diabetic ketoacidosis (DKA) in children, and to characterize AGNT as a criterion for DKA resolution in children admitted with moderate or severe disease. METHODS: A ten-year retrospective cohort study of children admitted to the intensive care unit with DKA. We used a survival analysis approach to determine changes in serum glucose, bicarbonate, pH, and anion gap following admission. Using multivariate analysis, we examined associations between patients' demographic and laboratory characteristics with delayed normalization of the anion gap. RESULTS: A total of 95 patients were analyzed. The median AGNT was 8 h. Delayed AGNT (>8 h) correlated with pH < 7.1 and serum glucose >500 mg/dL. In multivariate analysis, glucose >500 mg/dL was associated with an increased risk for delayed AGNT, by 3.41 fold. Each 25 mg/dL elevation in glucose was associated with a 10% increment in risk for delayed AGNT. Median AGNT preceded median PICU discharge by 15 h (8 vs. 23 h). DISCUSSION: AGNT represents a return to normal glucose-based physiology and an improvement in dehydration. The correlation observed between delayed AGNT and markers of DKA severity supports the usefulness of AGNT for assessing DKA recovery. Frontiers Media S.A. 2023-05-30 /pmc/articles/PMC10275565/ /pubmed/37334219 http://dx.doi.org/10.3389/fped.2023.1198581 Text en © 2023 Lazar, Wizeman-Orlov, Hazan, Orbach, Haim, Cavari, Feinstein, Neeman, Hershkovitz and Faingelernt. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Lazar, Isaac Wizeman-Orlov, Dorit Hazan, Guy Orbach, Asaf Haim, Alon Cavari, Yuval Feinstein, Yael Neeman, Eitan Hershkovitz, Eli Faingelernt, Yaniv The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis |
title | The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis |
title_full | The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis |
title_fullStr | The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis |
title_full_unstemmed | The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis |
title_short | The role of anion gap normalization time in the management of pediatric diabetic ketoacidosis |
title_sort | role of anion gap normalization time in the management of pediatric diabetic ketoacidosis |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275565/ https://www.ncbi.nlm.nih.gov/pubmed/37334219 http://dx.doi.org/10.3389/fped.2023.1198581 |
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